Canonical Allele Identifier: PA170597
Gene: HSD17B10 HGNC NCBI

Linked Data

ClinVar Variation Id: 144033
ClinVar RCV Id: RCV000133540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004484.1:p.Asp86Gly
CA170593
NM_004493.3:c.257A>G